| Literature DB >> 30338635 |
Ebin Sebastian1, Abbey M Philip1, Alfy Benny1, Mahesh Hariharan1.
Abstract
Exciton interactions in molecular aggregates play a crucial role in tailoring the optical behaviour of π-conjugated materials. Though vital for optoelectronic applications, ideal Greek cross-dipole (α=90°) stacking of chromophores remains elusive. We report a novel Greek cross (+) assembly of 1,7-dibromoperylene-3,4,9,10-tetracarboxylic tetrabutylester (PTE-Br2 ) which exhibits null exciton coupling mediated monomer-like optical characteristics in the crystalline state. In contrast, nonzero exciton coupling in X-type (α=70.2°, PTE-Br0 ) and J-type (α=0°, θ=48.4°, PTE-Br4 ) assemblies have perturbed optical properties. Additionally, the semi-classical Marcus theory of charge-transfer rates predicts a selective hole transport phenomenon in the orthogonally stacked PTE-Br2 . Precise rotation angle dependent optoelectronic properties in crystalline PTE-Br2 can have consequences in the rational design of novel π-conjugated materials for photonic and molecular electronic applications.Entities:
Keywords: charge mobility; chromophore aggregate; crystal engineering; exciton splitting; fluorescence
Year: 2018 PMID: 30338635 DOI: 10.1002/anie.201810209
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336